Product Recalls in Iowa

Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,447 recalls have been distributed to Iowa in the last 12 months.

49,990 total recalls
2,447 in last 12 months

Showing 2730127320 of 49,990 recalls

Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 125 DEG X Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 11X180 125DG STRL Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Merit Medical Systems, Inc.

Recalled Item: Flex-Neck Classic Peritoneal Dialysis Catheter (Pediatric) Product Usage: If...

The Issue: Mix-up between adult and pediatrics PD catheter.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN AR SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Boston Scientific Corporation

Recalled Item: SpyScope DS Access and Delivery diagnostic biliary catheter Recalled by...

The Issue: Certain lots of devices may have the working channel sleeve protruding from...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC END CAP STER TROC Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System TROCH NAIL ST 13X180 125DG STRL Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC NAIL 180X11X140 STER TROC Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD and and Xper FD ORT - Philips Recalled by Philips Electronics...

The Issue: Extra monitors, so called 7th or 8th monitor, mounted on the Monitor Ceiling...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Ad-Tech Medical Instrument Corporation

Recalled Item: Disposable Drill Kit which includes two drill bits Recalled by Ad-Tech...

The Issue: There is a possibility that DDK2-2.4-30X Disposable Drill Kits, Lot Number...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System STER TROC LAG SCR 70 MM Recalled by Zimmer...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 20, 2017· Zimmer Biomet, Inc.

Recalled Item: ACE Trochanteric Nail System ATN LAG SCREW 60MM STERILE ATN Recalled by...

The Issue: Zimmer Biomet is conducting a medical device recall for the ACE Trochanteric...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: CINtec PLUS Cytology Kit (CE-IVD) Recalled by Ventana Medical Systems Inc...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Cook Inc.

Recalled Item: Echosight Jansen-Anderson Intratubal Transfer Set Recalled by Cook Inc. Due...

The Issue: Certain lots of in vitro fertilization (IVF) products were distributed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: ultraView SISH DNP Detection Kit US Recalled by Ventana Medical Systems Inc...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: OptiView Amplification Kit Recalled by Ventana Medical Systems Inc Due to...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Implantable Cardioverter Defibrillators (ICDs) Recalled by Medtronic Inc.,...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Recalled by...

The Issue: Possible prevention of high and low voltage therapy in Medtronic Implantable...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: CINtec PLUS Cytology Kit (Canada/Japan) Recalled by Ventana Medical Systems...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing